Skip to main content
Nature genetics
CSK regulatory polymorphism is associated with systemic lupus erythematosus and influences B-cell signaling and activation.
Association of a functional variant downstream of TNFAIP3 with systemic lupus erythematosus.
Genome-wide association study meta-analysis identifies seven new rheumatoid arthritis risk loci.
Genetic variants at CD28, PRDM1 and CD2/CD58 are associated with rheumatoid arthritis risk.
A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus.
REL, encoding a member of the NF-kappaB family of transcription factors, is a newly defined risk locus for rheumatoid arthritis.
Common variants at CD40 and other loci confer risk of rheumatoid arthritis.
Multiple polymorphisms in the TNFAIP3 region are independently associated with systemic lupus erythematosus.
Genome-wide association scan in women with systemic lupus erythematosus identifies susceptibility variants in ITGAM, PXK, KIAA1542 and other loci.
PTPRC (CD45) is not associated with the development of multiple sclerosis in U.S. patients.
